Class II · Moderate risk
Heparin Sodium
Subpotent: Low anti-factor IIa Potency.
National Drug Code
Is NDC 0264-9587-20 recalled?
Heparin Sodium in Dextrose · 24 CONTAINER in 1 CASE (0264-9587-20) / 250 mL in 1 CONTAINER
Yes — this exact package was recalled
3 FDA recalls name the code 0264-9587-20 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Heparin Sodium and Dextrose
- Strength
- HEPARIN SODIUM 10000 [USP'U]/100mL; DEXTROSE MONOHYDRATE 5…
- Form
- Injection · Intravenous
- Labeler
- B. Braun Medical Inc.
- Type
- Human Prescription Drug
- Product code
- 0264-9587
Recalls naming this package
Class II · Moderate risk
Heparin Sodium
Subpotent Drug: low Anti-Factor IIa potency.
Class II · Moderate risk
Heparin Sodium 25
Subpotent Drug: low out-of-specification results were identified for the drug anti-factor IIa potency which is intended to ensure that the potency of heparin is within the USP specifications.
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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